Implants and methods for inter-spinous process dynamic stabilization of a spinal motion segment

ABSTRACT

An implant assembly for stabilizing a spinal motion segment includes a spacer which is at least partially flexible and positionable between adjacent spinous processes. The spacer member includes upper and lower surfaces structured to receive a respective adjacent one of the upper and lower spinous processes of the spinal motion segment and a body having flexibly distinctive first and second sections relative to one another configured to modify the manner of movement at the spinal motion segment.

BACKGROUND

Implants can be positioned between adjacent spinous processes to provideresistance to vertebral movement as a result of extension of the spinalcolumn. These implants can provide a shock absorber or bumper thatdynamically limits spinal extension. The implants can be secured to theadjacent spinous processes with looped cables or straps that extendcompletely about the spinous processes and implant to maintainpositioning of the implant between the spinous processes while alsolimiting spinal flexion. However, in addition to controlling the rangeof motion between adjacent spinal motion segments, it has beendiscovered that more positive patient outcomes also rely on changing themanner in which the adjacent spinal motion segments move relative toeach other. Thus, there remains a need for an implant which can bothcontrol motion and alter the manner in which the spinal motion segmentsmove.

SUMMARY

There is provided spinal implants, implant assemblies and methods thatprovide stabilization of a spinal motion segment through the posteriorvertebral elements.

According to one aspect, a spinal implant includes a spacer member whichextends along a longitudinal axis between opposite upper and lower ends.The upper and lower ends are structured to receive a respective one ofthe adjacent upper and lower spinous processes of a spinal motionsegment. The spacer member includes a body including at least a firstand a second section. Each of the first and second sections includes aflexibility characteristic that is different from the other.

According to another aspect, a spinal implant includes a spacer sizedand shaped to extend between adjacent upper and lower spinous processesof a spinal motion segment. The spacer member includes a body with anexterior wall extending between opposite upper and lower ends. In animplantation orientation between the upper and lower spinous processes,the exterior wall includes an anterior surface opposite a posteriorsurface. The body further includes at least a first section having afirst flexibility characteristic quality and a second section having asecond flexibility characteristic that differs from the firstflexibility characteristic. In one form, the first and second sectionsare configured to modify the manner of movement of the spinal motionsegment when implanted between spinous processes of the adjacentvertebrae.

According to a further aspect, a method for stabilizing a spinal motionsegment comprises: providing a spacer member including an upper endstructured to contact an inferior surface of the upper spinous processand a lower end structured to contact a superior surface of the lowerspinous process and a body including at least flexibly distinctive firstand second sections, with the first section being less flexible than thesecond section; and positioning the spacer member between the adjacentupper and lower spinous processes of the spinal motion segment with thefirst section oriented anteriorly.

These and other aspects will be discussed further below.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an elevation view of a posterior portion of a spinal columnmotion segment with a spinal implant in the form of a spacer memberengaged therewith.

FIG. 2 is a lateral view of the spinal column motion segment of FIG. 1.

FIGS. 3A-3G are sectional views taken along view line 3-3 of FIG. 1 ofvarious alternative embodiment spacer members.

FIG. 4 is a sectional view of the spacer member of FIGS. 1 and 2 takenalong view line 4-4 in FIG. 2.

FIG. 4A is a sectional view of an alternative embodiment spacer membertaken along a view plane corresponding to line 4-4 in FIG. 2.

FIG. 4B is a sectional view of an alternative embodiment spacer membertaken along a view plane corresponding to line 4-4 in FIG. 2.

FIG. 5 is a perspective view of an alternative embodiment spacer member.

FIG. 6 is a sectional view taken along view line 6-6 in FIG. 5.

FIG. 7 is a perspective view in partial section of another embodimentspacer member.

FIG. 8 is an elevation view of the posterior portion of the spinalcolumn motion segment of FIG. 1 with a spacer member assembly includinga tethering system engaged therewith.

FIG. 9 is a lateral view of the spinal column motion segment and spacermember assembly of FIG.8.

FIGS. 10A-10C are sectional views taken along view line 10-10 in FIG. 8of various alternative embodiment spacer members.

DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS

For the purposes of promoting an understanding of the principles of theinvention, reference will now be made to the embodiments illustrated inthe drawings and specific language will be used to describe the same. Itwill nevertheless be understood that no limitation of the scope of theinvention is thereby intended. Any such alterations and furthermodifications in the illustrated devices, and such further applicationsof the principles of the invention as illustrated herein arecontemplated as would normally occur to one skilled in the art to whichthe invention relates.

Implants are positionable between adjacent spinous processes of a spinalmotion segment to dynamically stabilize and limit spinal extensionand/or flexion while altering the manner of movement between adjacentvertebral bodies which in one form includes repositioning the center ofrotation for one or both of flexion and extension movement at the spinalmotion segment. The implant includes a spacer member that forms acomposite structure received between the spinous processes. The implantincludes at least a first section and a second section with aflexibility characteristic that differs from that of the first section.In one form, the configuration of the first and second sections providesan asymmetry of flexibility between anterior and posterior sides of theimplant that provides preferential deformation and influences therepositioning of the centers of rotation for flexion and extension atthe spinal motion segment. In another form, the spacer member may beemployed alone or with other implants, such as rods, plates, tethers,interbody fusion devices, interbody spacers, artificial discs, annulusrepair system, or staples, for example.

In a further form, one or more engaging members in the form of a tethercouples the implant to one or more posterior vertebral elements orimplants. The engaging members can be engaged to the spacer member, orextend through the spacer member. The engaging members can be engaged tothe posterior elements in a configuration that at least partially limitsspinal flexion. Alternatively or additionally, the engaging members canbe engaged to the posterior elements in a manner that prevents orresists the spacer member from being displaced from its implantationlocation between the spinous processes. In yet another form, theengaging members may increase the rigidity of one or more of the firstand second sections.

In FIGS. 1 and 2 there is shown a spinal column segment 10 including anupper vertebra V_(U), a lower vertebra V_(L) and a spinal disc 13therebetween along a central axis 11 of the spinal column. The vertebraeV_(U), V_(L) and disc 13 comprise a spinal motion segment, it beingunderstood that a spinal motion segment may include multiple vertebrallevels in one more of the lumbar, thoracic, and cervical regions of thespine. Upper vertebra V_(U) includes an upper spinous process SP₁ whilethe lower vertebra V_(L) includes a lower spinous process SP₂, with thespinous processes SP₁, SP₂ defining a space S therebetween. The spinousprocesses SP₁ and SP₂ comprise posterior elements of the vertebraeV_(U), V_(L) of the spinal motion segment along with the transverseprocesses 15, 16, 17, and 18, laminae 19 a, 19 b, facets, pedicles andother posterior structures of each vertebrae V_(U), V_(L).

A spinal implant 30 in the form of a spacer member 31 is positioned inthe space S and extends between and engages with the spinous processesSP₁, SP₂ to provide stabilization and modification of the spinal motionsegment. Spacer member 31 includes a body 32 which in its implantedorientation has a first lateral side 34 and a second lateral side 36,with the lateral sides 34, 36 extending between a superior end 38 and aninferior end 40. As best seen in FIG. 2, for example, the body alsoincludes an anterior side 42 opposite a posterior side 44. It should beappreciated that the transition between each of the anterior andposterior sides 42, 44, lateral sides 34, 36, and superior and inferiorends 38, 40 may be rounded or beveled in order to decrease the profileof the body 32 and minimize intrusion and potential trauma to adjacentneural tissue and surrounding spinal anatomy.

The body 32 further includes a first concave portion 46 and a secondconcave portion 48 situated at respective superior and inferior ends 38,40. Each of the concave portions 46, 48 is disposed between a pair ofrespective upright arms 50 a, 50 b and 52 a, 52 b. Concave portions 46,48 are sized and shaped to engage with and receive respective inferiorsurface 12 of the upper spinous process SP₁ and superior surface 14 ofthe lower spinous process SP₂. The arms 50 a, 50 b, 52 a, and 52 bextend beyond the respective concave portions 46, 48 to engage with thelateral sides of the spinous processes SP₁, SP₂. While concave portions46, 48 are illustrated having a substantially arcuate shape, it shouldbe appreciated that in one or more forms the concave portions 46, 48 mayinclude an alternative configuration, such as a rectangular shape or maybe structured to receive a greater portion of the spinous processes SP₁,SP₂ to further resist dislodgement from space S.

As illustrated in FIG. 2, the upper vertebra V_(U) and lower vertebraV_(L) have a normal center of rotation COR_(N) (illustrated in phantom)for flexion and extension motion of the spinal motion segment when thespacer member 31 is not positioned in space S between the spinousprocesses SP₁, SP₂. While the normal center of rotation COR_(N) islocated substantially in the center of the vertebral bodies VB₁, VB₂ inFIG. 2, it should be appreciated that the position of the normal centerof rotation COR_(N) may vary based on several factors, including theregion of the spinal column, individual patient anatomy, disease stateor the effects of concurrent procedures (such as spinal decompression),just to name a few. Also illustrated in FIG. 2 are the resultantpositions for the center of rotation for flexion COR_(F) and the centerof rotation for extension COR_(E) when one form of spacer member 31according to the present application is inserted in space S between thespinous processes SP₁, SP₂. In this form, the center of rotation forflexion COR_(F) is repositioned anterior to the normal center ofrotation COR_(N) while the center of rotation for extension COR_(E) isrepositioned posterior to the normal center of rotation COR_(N). Furtherdetails in regard to modifying the normal center of rotation COR_(N)will be set forth below.

Referring now to FIG. 3A there is shown a sectional view of oneembodiment spacer member 31 along line 3-3 of FIG. 1. In thisembodiment, the spacer member includes a first section 54 adjacent toanterior side 42 and a second section 56 positioned adjacent toposterior side 44 and abutting against first section 54, with each ofthe sections 54, 56 extending longitudinally between the spinousprocesses SP₁, SP₂. A portion of first section 54 is surrounded, atleast along its superior and inferior sides, with second section 56.First and second sections 54, 56 form an overlapping arrangement in theanterior-posterior directions that provides a transition in thestiffness profile where the stiffness decrease posteriorly. Firstsection 54 includes a posterior portion 55 that extends part-way intosecond section 56 in the anterior to posterior direction.

In this and the other forms contemplated herein, the spacer member 31 isfabricated from components that are flexible or exhibit at least someflexibility with the second section 56 being more flexible than thefirst section 54. Additionally, at least a portion of the spacer member31 is resilient and/or elastic so it can assume various shapes duringand after insertion and attachment. In one form, the flexibility of oneor both of sections 54 and 56 is controlled by constructing the spacermember 31 with longitudinal gradations. In another form, the flexibilityof the sections 54, 56 is varied by using materials with differentelasticity, flexibility, or rigidity qualities. In one form, it iscontemplated that the materials for the first section 54 and the secondsection 56 are selected based upon their modulus of elasticity.

It should be appreciated that either of sections 54, 56 may comprise anybiocompatible material, material of synthetic or natural origin, andmaterial of a resorbable or non-resorbable nature so long as theflexibility of the sections varies. For example, in one form of thepresent application, section 54 comprises PEEK while section 56comprises silicone. It is also contemplated that other polymers such asultra-high molecular weight polyethylene, polyaryletherketone,polyacetal, polysulfone, polyimide, polyester, polyvinyl alcohol,polyacrylonitrile, polytetrafluorethylene, poly-paraphenylene,terephthalamide, cellulose, biocompatible rubber materials, andcombinations thereof may be used. Suitable ceramic materials may includealumina, zirconia, polycrystalline diamond compact, pyrolitic carbon,and porous tantalum material. Suitable composite materials may includecarbon-filled composites, hydroxyl-appetite-filled composites, andbioactive-glass-filled composites. The spacer member 31 may also includeautograft, allograft or xenograft material and tissue materialsincluding soft tissues, connective tissues, demineralized bone matrixand combinations thereof. In an embodiment including a resorbablematerial, any one or more of polylactide, polyglycolide,tyrosine-derived polycarbonate, polyanhydride, polyorthoester,polyphosphazene, calcium phosphate, hydroxyapatite, bioactive glass,collagen, albumin, fibrinogen and combinations thereof may be a suitablematerial. It should be appreciated that the selection of material forone or both of sections 54, 56 will influence the positioning of thecenters of rotation for flexion and extension COR_(F), COR_(E).

When spacer member 31 is inserted into the space S each of the spinousprocesses SP₁, SP₂ bears against the first section 54 and the moreflexible second section 56. Since the spinous processes bear againstboth sections 54 and 56, a preferential deformation of the spacer member31 is formed by movement of the spinal motion segment and the centers ofrotation for flexion and extension COR_(F), COR_(E) are influenced. Whenthe more rigid section 54 is disposed anterior to the second section 56and the spinal motion segment undergoes extension, the center ofrotation for extension COR_(E) is moved posterior to the normal centerof rotation COR_(N) because the spinous processes SP₁, SP₂ rotate aboutthe more rigid section 54 and compress or deform the more flexiblesecond section 56 as they move toward one another. As the spinal motionsegment undergoes flexion movement, the spinous processes SP₁, SP₂ againrotate about the more rigid section 54 until enough force is created tocompress or deform section 54, thus repositioning the center of rotationfor flexion COR_(F) anterior to the normal center of rotation COR_(N).Moreover, when the more rigid section 54 is placed anterior to thesecond section 56, section 54 is provided with sufficient rigidity inone embodiment to maintain a distraction distance between the laminae 19a, 19 b in order to avoid stenosis and associated neural complications.

Referring now generally to each of FIGS. 3B-3G there is illustrated asectional view of alternative embodiment spacer members 31 b-31 g. Itshould be understood that the configuration of each of the spacermembers 31 a-31 g has been varied by adjusting the positioning of thefirst section 54 relative to the second section 56 in order to providespacer members with alternative flexibility characteristics which may beused to alternatively vary or control movement of the spinal motionsegment.

Referring to FIG. 3B, spacer member 31 b further includes a thirdsection 58 which comprises a material generally more flexible than thematerial of sections 54, 56. The material of section 58 is generallystructured to conform to the respective adjacent spinous process SP₁ orSP₂ in order to provide enhanced reception and engagement and maycomprise one or more of the materials suitable for sections 54 and 56.For example, in FIGS. 3C and 3D the spacer members 31 c and 31 d willreact much the same as spacer 31 during flexion and extension. In FIG.3C, first section 54 and second section 56 are arranged in side-by-siderelation to one another in the anterior-posterior direction with nooverlapping portions. In FIG. 3D, first section 54 includes a posteriorextension 55 that is surrounded at least one its superior and inferiorsides with second section 56, and extension 55 extends to the posteriorside 44.

In FIG. 3E, the first section 54 is disposed both superiorly andinferiorly around the second section 56, such that the first section 54creates an axial force which compresses the second section 56 duringextension of the spinal motion segment. Moreover, in FIG. 3F the firstsection 54 of spacer member 31f is at least partially surrounded by thesecond section 56 such that the first section 54 will limit theflexibility of the second section 56 when a force greater than theelastic or compressive limit of section 56 is applied thereto. In FIG.3G, first section 54 is surrounded at least partially along its anteriorand posterior sides with a more flexible second section 56. Spacer 31gwill provide deformation of the second section 56 during both spinalextension and spinal flexion, while first section 54 provides resistanceto deformation when the supported vertebrae are in their neutralposition.

In the embodiments discussed above, the arrangement of the first andsecond sections can be reversed so that the first section 54 is moreflexible than the second section 56. Still other embodiments contemplatemore than first and second sections to provide additional gradations inthe flexibility of the implant. In still other embodiments, it iscontemplated that one of the first and second sections may be removablefrom the spacer member and replaced with an alternative replacementsection in order to alter the flexibility characteristics of the spacermember. For example, in the embodiment illustrated in FIG. 3A, secondsection 56 may be removable from the spacer member 31. A plurality ofreplacement sections having flexibility characteristics different fromthe first section 54 and the second section 56 may be provided toreplace the second section 56. It should be appreciated that both thesecond section 56 and the replacement sections may be engaged with thespacer member 31 and the first section 54 through any standard manner,including a friction fit, pinning, tacking, stapling, screwing and/orany combination thereof, just to name a few possibilities. In this form,the stabilization of the spinal motion segment may be monitoredsubsequent to positioning the spacer member 31 between the spinousprocesses SP₁, SP₂ to determine if alterations to the stabilization aredesired. For example, it may be desired to adjust the positioning of oneor both of the centers of rotation for flexion and extension COR_(F),COR_(E). When an alteration to the stabilization of the spinal motionsegment is desired, the removable section may be replaced with one ofthe replacement sections having different flexibility characteristics.For example, in one non-limiting form, when it is desired to repositionthe center of rotation for extension COR_(E) in an anterior direction,the flexibility of the selected replacement section may be less thanthat of the second section 56 but greater than that of the first section54. It should be appreciated that the stabilization of the spinal motionsegment may be continually monitored and that the removable one of thefirst and second sections may be replaced with one of the replacementsections until the desired stabilization is achieved. The procedure ofremoving the removable section and replacing it with the alternativesection may be performed through any standard surgical procedure.However, in one form, in order to minimize surgical complexity andtrauma to the patient, it is contemplated that the procedure isperformed percutaneously through a minimally invasive procedure.

Referring now to FIGS. 4A and 4B, wherein like numerals refer to likefeatures previously described, there is shown a sectional view ofrespective spacer members 31 and 31 b along line 4-4 of FIG. 2. In FIG.4A, the portion of the body 32 of spacer member 31 which forms arms 50a, 50 b, 52 a, and 52 b engages with the upper and lower spinousprocesses SP₁, SP₂. In one form, this portion of the body 32 may beflexible enough to at least partially conform to the spinous processesSP₁, SP₂. In an alternative embodiment such as spacer 31 b, the thirdsection 58 is disposed around the concave portions 46 b, 48 b to providea surface that conforms to the spinous processes SP₁, SP₂ regardless ofthe flexibility or rigidity of the rest of the body 32 b.

An alternative embodiment spinal implant 70 in the form of spacer member71 is illustrated in perspective view in FIG. 5. The spacer member 71includes a substantially U-shaped body 73 including longitudinal members75 and 76 and an arcuate portion 82 extending between the longitudinalmembers 75, 76 to form a concave area 84 extending between surfaces 78and 80. In an implantation orientation the body 72 is structured forpositioning in the space S between the upper and lower spinous processesSP₁, SP₂ such that the concave area 84 faces in an anterior directionwith the upright members 75, 76 abutting a posterior surface of thelaminae 19 a, 19 b and the upper spinous process SP₁ engaging withsurface 78 and the lower spinous process SP₂ engaging with surface 80.In one non-illustrated embodiment, the body 72 may be structured so thatthe longitudinal members 75, 76 may be positioned between the adjacentlaminae 19 a, 19 b to keep a distraction space between the laminae 19 a,19 b while the surfaces 78, 80 engage with and support the adjacentspinous processes SP₁, SP₂. In one or more forms, the body 72 mayinclude one or more features structured to resist anterior migration ofthe implant 70 into the spinal canal. In yet another non-illustratedform, it is contemplated that surfaces 78, 80 may include a recessedarea for receiving and engaging the spinous process SP₁, SP₂.

Referring to FIG. 6, there is shown a section view of the spacer member71 along view line 6-6 of FIG. 5. In this form, spacer member 71includes a first section 86 disposed generally in the longitudinalmembers 75, 76 and a second section 88 disposed generally in the arcuateportion 82. As described above in regard to spacer member 31, the spacermember 71 can be fabricated from components that are flexible or exhibitat least some flexibility with the second section 88 being more flexiblethan the first section 86. In one form, the flexibility of the sections86, 88 may be varied by using materials with different elastic,flexibility, or rigidity qualities. It is further contemplated that oneor more of the materials comprising sections 86, 88 may be selected fromthe materials set forth herein above in regard to spacer member 31. Inthe implantation orientation of spacer member 71, the more rigid firstsection 86 is positioned anterior to the more flexible second section 88and the centers of rotation for flexion and extension COR_(F), COR_(E)will be repositioned relative to the normal center of rotation COR_(N)as described above in regard to spacer member 31. Moreover, with themore rigid section 86 disposed generally in longitudinal members 75, 76,the spacer member 71 will maintain a distraction distance between thelaminae 19 a, 19 b to help avoid stenosis and associated neuralcomplications. While alternative section views of spacer member 71 havenot been provided, it is contemplated that the configuration andpositioning of the first section 86 and the second section 88 may bemodified in order to provide a spacer member 71 with various flexibilityand stabilization features.

An additional alternative embodiment spinal implant 100 in the form ofspacer member 101 is illustrated in perspective view in FIG. 7. Spacermember 101 is generally similar to spacer member 31 and includes a body102 which in an implantation orientation extends between a superior end104 and an inferior end 106. The body 102 also generally includeslateral sides 108, 110 and anterior side 112 and posterior side 114. Theconcave portions 116, 118 are structured to engage with and receive theupper and lower spinous processes SP₁, SP₂ as described herein. In theillustrated form, the body includes a first section 120 positionedanterior to a hollow chamber 122 with the chamber 122 being structuredto receive one or more injectable materials. When the chamber 122includes the injectable material, the body 102 includes a second sectionin addition to the first section 120. The injectable material mayinclude gels, pastes, slurries, or liquids, just to name a fewpossibilities. In one form, the injectable material may be deliverablein a first state and cure to a second state after injection. However,regardless of the form, the injectable material will be more flexiblethan the first section 120 in order to provide an implant withflexibility and stabilization features similar to that of spacer member31. In one non-illustrated form, the body 102 may include one or moreinjection ports to receive the injectable material from a deliveryinstrument. In yet another form, it is contemplated that the body 102may include one or more chambers in addition to chamber 122. It shouldalso be appreciated that the positioning of the one or more chambers 122or first section 120 may be altered to provide spacer members withvarious flexibility and stabilization features. Moreover, it iscontemplated that section 120 may be the more flexible section and thatthe more rigid material may be delivered to the one or more chambers122.

In another form, it is contemplated that the injectable material may beremoved from the chamber 122 subsequent to positioning of the spacermember 101 at an implantation location. In this form, a patient may bemonitored to determine if changes to the stabilization of the spinalmotion segment are necessary. For example, after the initial positioningof the spacer member 101, it may be determined that one or both of thecenters of rotation for flexion and extension COR_(F), COR_(E) needs tobe adjusted. If an adjustment is necessary, the injectable material maybe removed and replaced with an alternative injectable material havingdifferent flexibility characteristics in order to alter one or both ofthe centers of rotation for flexion and extension COR_(F), COR_(E) asdesired. It is further contemplated that the stabilization of the spinalmotion segment may be continuously monitored and, if necessary, theinjectable material may be varied until desired stabilization of thespinal motion segment is accomplished. The injectable material may beremoved and introduced to the chamber 122 of the spacer member 101through any known surgical procedure. In one form however, the spacermember 101 is structured for access by a delivery instrument through apercutaneous surgical procedure in a minimally invasive manner in orderto minimize surgical complexity and trauma to the patient.

Referring now to FIGS. 8 and 9, there is shown an implant assembly 125relative to the spinal motion segment of FIGS. 1 and 2. Implant assembly125 includes a spinal implant 130 in the form of a spacer member 131positioned in the space S and extending between and engaging with thespinous processes SP₁, SP₂ to provide stabilization and modification ofthe spinal motion segment. Spacer member 131 includes a body 132 whichin its implanted orientation has a first lateral side 134 and a secondlateral side 136, with the lateral sides 134, 136 extending between asuperior end 138 and an inferior end 140. As best seen in FIG. 9, forexample, the body also includes an anterior side 142 opposite aposterior side 144. It should be appreciated that the transition betweeneach of the anterior and posterior sides 142, 144, lateral sides 134,136, and superior and inferior ends 138, 140 may be rounded or beveledin order to decrease the profile of the body 132 and minimize intrusionand the potential for trauma to adjacent neural tissue and surroundingspinal anatomy.

The body 132 further includes a first concave portion 146 and a secondconcave portion 148 situated at respective superior and inferior ends138, 140. Each of the concave portions 146, 148 is disposed between apair of respective upright arms 150 a, 150 b and 152 a, 152 b. Concaveportions 146, 148 are sized and shaped to engage with and receiverespective inferior surface 12 of the upper spinous process SP₁ andsuperior surface 14 of the lower spinous process SP₂. The arms 150 a,150 b, 152 a, and 152 b extend beyond the respective concave portion 146and concave portion 148 to engage with the lateral sides of the spinousprocesses SP₁ , SP₂ to prevent or resist dislodgement of the spacermember 131 from space S.

Spacer member 131 is similar to spacer member 31 discussed above butalso includes an engaging member 160 extending therefrom to attachspacer member 131 to posterior vertebral elements or implants of thespinal motion segment. Spacer member 131 includes any arrangement forspacer member 31 discussed above in FIGS. 1-3G. Spacer member 131includes through-passages 162 extending between opposite sides thereof,which include the lateral sides 134, 136 of spacer member 131 in theillustrated embodiment. Passages 162 receive engaging member 160therethrough. Engaging member 160 may comprise multiple engagingmembers, or a single engaging member looped through passages 162. Stillother embodiments contemplate a single passage 162, or three or morepassages 162, through which one or more engaging members 160 arepositioned.

Referring to FIG. 10A there is illustrated a section view of spacermember 131 along view line 10-10 of FIG. 8. As indicated, spacer member131 is similar to spacer member 31 and likewise includes a first section154 and a more flexible second portion 156. Sections 154, 156 are alsosimilar to sections 54, 56 described above in regard to spacer 31.However, the first section 154 includes passages 162 extendingtherethrough. When the engaging member 160 is received in passages 162and is engaged to posterior vertebral elements or other implants and anaxial pulling force is exerted on the spacer member 131, the more rigidsection 154 resists deformation of the spacer body. Moreover,alternative embodiment spacer members 131 b and 131 c are illustrated insection view in FIGS. 10B and 10C. In FIG. 10B, the passages extendthrough the more rigid section 154 such that as an axial pulling forceis exerted on the spacer member 131 b, the more rigid section 154 againresists deformation of the spacer member 131 b. In FIG. 10C, thepassages 162 extend through the more flexible second section 156 whichis situated between superior and inferior portions of first section 154.In this form, the second section 156 is deformable in response to theaxial pulling force until it is limited by the surrounding more rigidfirst section 154. It should be appreciated that the engaging member 160and the passages 162 may be alternatively configured relative to thefirst and second sections 154, 156 in accordance with the variousembodiments set forth herein.

Engaging member 160 can be in the form of a tether, cord, wire, cable,suture, band, strap, belt, or other suitable structure for manipulationand securement to one or more posterior vertebral elements. Engagingmember 160 may be wrapped or positioned around posterior vertebralelements and then maintained in position with a crimp or other suitablefastener. Furthermore, engaging member 160 can be coupled to spacermember 131 in any suitable manner. In one embodiment, engaging member160 is movably coupled to spacer member 131. Engaging member 160 can beintegrally formed with spacer member 131, or can be attached by afastener, suture, anchor, cable, link, over-molding or other suitableconnection. Spacer member 131 can be provided with ears, eyelets,recesses or other suitable structure to facilitate engagement ofengaging member 160 to spacer member 131. Engaging member 160 may beemployed in spinal stabilization procedures where it is desired to limitspinal flexion by, for example, wrapping engaging member 160 about thesuperior surface of the upper spinous process and/or upper lamina andthe inferior surface of the lower spinous process and/or the lowerlamina. Engaging member may alternatively be employed as a retentionmechanism to maintain spacer member 160 in position between the spinousprocesses.

With respect to the various embodiments described herein, the engagingmember can be joined or fixed to the spacer member using various devicesand/or techniques, or can be integrally formed with or form an extensionof the spacer member. The spacer member can be joined or attached to theengaging member by, for example, sewing the engaging member to thespacer member, thermal welding or bonding, adhesive bonding, threedimensional weaving or braiding, screws, staples, pins, tacks or rivetfixation. Furthermore, the engaging member can be secured to the spacermember either before or after the spacing member is placed between thespinous processes. The engaging member can be engaged to other engagingmembers of other implant assemblies or to other implants engaged to thespinal column in the surgical procedure.

The engaging members described herein can be made from any one orcombinations of biocompatible material, including synthetic or naturalautograft, allograft or xenograft tissues, and can be resorbable ornon-resorbable nature. Examples of tissue materials include hardtissues, connective tissues, demineralized bone matrix and combinationsthereof. Further examples of resorbable materials are polylactide,polyglycolide, tyrosine-derived polycarbonate, polyanhydride,polyorthoester, polyphosphazene, calcium phosphate, hydroxyapatite,bioactive glass, and combinations thereof. Further examples ofnon-resorbable materials are carbon-reinforced polymer composites,shape-memory alloys, titanium, titanium alloys, cobalt chrome alloys,stainless steel, and combinations thereof.

While not illustrated, it should be appreciated that one or more of thespacers contemplated herein may include one or more additional sectionswith one more additional elasticity, flexibility, or rigidity qualities.Moreover, in another non-illustrated form, it is contemplated that uponimplantation the spacer member may not include one of the first orsecond sections. In this form, a plurality of coupleable members sizedand shaped like the first or second section may be provided withdiffering flexibility characteristics so that a surgeon may select whichto include at the implant site during a surgical procedure. It should beappreciated that the coupleable members may engage with the spacermembers through any one or more of a press fit engagement, a mechanicalconnection, fusion, or adhesion, just to name a few possibilities. Itshould also be appreciated that in one or more forms the spacer membersmay be integrally formed or may include one or more portions coupledtogether.

In a further embodiment, it is contemplated that stiffening members canbe provided to enhance or increase the stiffness of spacer members 31,71, 101, 131. For example, in one non-illustrated form, a stiffeningmember may be in the form of a band that extends about and contacts theperimeter of spacer members 31, 71, 101, 131. Moreover, more than onestiffening member can be provided about spacer members 31, 71, 101, 131to allow the stiffness profile of the spacer members 31, 71, 101, 131 tobe increased or decreased by adding or removing a stiffening member.Examples of suitable stiffening members include woven fabric tubing,woven and non-woven mesh, or braided or woven structures, sutures,tethers, cords, planar members, bands, wires, cables, or any othercomponent capable of extending about the perimeter of the spacer memberto increase stiffness thereof.

While the invention has been illustrated and described in detail in thedrawings and foregoing description, the same is to be consideredillustrative and not restrictive in character, it being understood thatonly selected embodiments have been shown and described and that allchanges, equivalents, and modifications that come within the scope ofthe inventions described herein or defined by the following claims aredesired to be protected. Any experiments, experimental examples, orexperimental results provided herein are intended to be illustrative ofthe present invention and should not be construed to limit or restrictthe invention scope. Further, any theory, mechanism of operation, proof,or finding stated herein is meant to further enhance understanding ofthe present invention and is not intended to limit the present inventionin any way to such theory, mechanism of operation, proof, or finding. Inreading the claims, words such as “a”, “an”, “at least on”, and “atleast a portion” are not intended to limit the claims to only one itemunless specifically stated to the contrary. Further, when the language“at least a portion” and/or “a portion” is used, the claims may includea portion and/or the entire item unless specifically stated to thecontrary.

1. A spinal implant, comprising: a spacer member extending along alongitudinal axis between opposite upper and lower ends, said upper andlower ends being structured to receive a respective adjacent one ofupper and lower spinous processes of a spinal motion segment, saidspacer member including a body with at least a first section and asecond section structured for positioning between and in supportingengagement with the upper and lower spinous processes, said first andsecond sections including flexibility characteristics that differ fromone another.
 2. The implant of claim 1, wherein said first sectionincludes a first material and said second section includes a secondmaterial, with said second material being more flexible than said firstmaterial.
 3. The implant of claim 1, wherein said flexibilitycharacteristic relates to a modulus of elasticity and wherein saidsecond section has a smaller modulus of elasticity than said firstsection.
 4. The implant of claim 3, wherein each of said upper and lowerends includes a concave portion sized and shaped to receive one of therespective upper and lower spinous processes, said concave portionsbeing disposed between a pair arms extending from said upper and lowersurfaces to engage with lateral surfaces of the spinous processes. 5.The implant of claim 4, wherein said spacer member includes a posteriorsurface and an anterior surface in an implantation orientation betweenthe upper and lower spinous processes, said anterior and posteriorsurfaces extending between said upper and lower ends and wherein saidfirst section is positioned adjacent said anterior surface and saidsecond section is positioned adjacent said posterior surface.
 6. Theimplant of claim 4, wherein said body further includes a third sectiondisposed adjacent to said concave portions, said third section beingstructured to conform to the upper and lower spinous processes when theupper and lower spinous processes bear against said concave portions. 7.The implant of claim 1, wherein said first section of said body includesa first longitudinal member and a second longitudinal member and saidsecond section includes a partially arcuate portion disposed betweensaid first and second members such that said body is substantiallyU-shaped, said arcuate portion including first and second surfacesstructured to receive a respective adjacent one of the upper and lowerspinous processes and said first and second longitudinal members beingstructured to engage with upper and lower Is laminae of the spinalmotion segment.
 8. The implant of claim 7, wherein said characteristicrelates to a modulus of elasticity and wherein said second section has asmaller modulus of elasticity than said first section.
 9. The implant ofclaim 1, further comprising at least one tether engaged to said body andextending therefrom, said tether being engageable with one of the upperand lower spinous processes.
 10. The implant of claim 9, wherein said atleast one tether extends through said first section and wherein saidfirst section is more rigid than said second section.
 11. The implant ofclaim 10, wherein said first section includes at least one boreextending therethrough between opposite sides of said body transverselyto a direction between said upper and lower ends, said at least onetether extending through said at least one bore.
 12. The implant ofclaim 11, further comprising a second bore through said first section ofsaid body adjacent to and paralleling said first bore.
 13. The implantof claim 12, further comprising a second tether extending through saidsecond bore, said second tether being engageable with the other of theupper and lower spinous processes.
 14. The implant of claim 9, whereinsaid at least one tether extends through said second section of saidbody, said second section being less rigid than said first section andbeing at least partially surrounded by said first section.
 15. A spinalimplant, comprising: a spacer sized and shaped to extend betweenadjacent upper and lower spinous processes of a spinal motion segment,said spacer member including a body with an exterior wall extendingbetween opposite upper and lower ends, said exterior wall including aposterior surface and an anterior surface when in an implantationorientation between the upper and lower spinous processes and said bodyincluding at least a first section means having a first flexibilitycharacteristic for movably supporting the upper and lower spinousprocesses when positioned therebetween and a second section means havinga second flexibility characteristic for movably supporting the upper andlower spinous processes when positioned therebetween that differs fromsaid first flexibility characteristic.
 16. The implant of claim 15,wherein said second flexibility characteristic of said second sectionmeans is defined by a smaller modulus of elasticity than a modulus ofelasticity of said first section means.
 17. The implant of claim 15,wherein said first section means comprises a first material and saidsecond section means comprises a second material, said second materialbeing more flexible than said first material.
 18. The implant of claim15, wherein said first section means extends from said anterior surfacetoward said posterior surface and said second section means extends fromsaid posterior surface toward said anterior surface.
 19. The implant ofclaim 18, wherein said first section means includes a posteriorextension that is at least partially surrounded by said second sectionmeans.
 20. The implant of claim 18, wherein said first section meansextends along upper and lower sides of said second section means. 21.The implant of claim 15, wherein said first section means extendssubstantially parallel to said anterior and posterior surfaces and saidsecond section means extends along anterior and posterior sides of saidfirst section means.
 22. The implant of claim 15, wherein said firstsection means and said second section means extend between extendbetween said anterior and posterior surfaces and said second sectionmeans extends along upper and lower sides of said first section.
 23. Theimplant of claim 15, wherein said upper and lower surfaces include aconcave portion structured to receive one of said respective upper andlower spinous processes.
 24. The implant of claim 23, wherein said bodyfurther comprises a third section disposed adjacent said concaveportions, said third section comprising a compressible materialstructured to conform to the respective adjacent upper and lower spinousprocesses when the spinous processes bear against said concave portions.25. The implant of claim 23, wherein each of said upper and lowersurfaces includes a pair of arms extending therefrom to engage withlateral surfaces of one of said respective upper and lower spinousprocesses.
 26. The implant of claim 15, wherein at least one of saidfirst and second section means defines an internal chamber including aninjectable material disposed therein, said injectable material having adifferent modulus of elasticity than the other of the first and secondsection means.
 27. The implant of claim 15, further comprising at leastone tether engaged to said body and extending therefrom, said tetherbeing engageable with one of the upper and lower spinous processes. 28.A method for stabilizing a spinal motion segment, comprising: providinga spacer member including an upper end structured to contact an inferiorsurface of an upper spinous process and a lower end structured tocontact a superior surface of a lower spinous process and a bodyincluding at least flexibly distinctive first and second sectionsforming an asymmetrical stiffness profile that varies between anteriorand posterior sides of said body; and positioning said spacer memberbetween the upper and lower spinous processes of the spinal motionsegment with said first section oriented anteriorly and said secondsection oriented posteriorly and with said first and second sectionsmovably supporting the upper and lower spinous processes.
 29. The methodof claim 28, wherein said spacer member varies the center of rotationfor flexion and extension of an upper vertebral body engaged to saidupper spinous process relative to a lower vertebral body engaged to saidlower spinous process.
 30. The method of claim 28, further comprisingpositioning each of the upper and lower spinous processes between armsat each of the upper and lower ends of the spacer member.
 31. The methodof claim 28, further comprising engaging the spacer member to posteriorvertebral elements of the spinal motion segment with a tether.
 32. Themethod of claim 28, further comprising providing additional spacermembers including alternative configurations defined by the positioningof said first section relative to said second section, wherein saidfirst section is less rigid than said second section in each of saidadditional spacer members.
 33. The method of claim 28, furthercomprising injecting a first injectable material into a chamber in oneof the first and second sections, the injectable material including amodulus of elasticity different from that of the other first or secondsection.
 34. The method of claim 33, further comprising: monitoring thestabilization of the spinal motion segment subsequent to the injectingof the first injectable material; removing the first injectable materialfrom the chamber of the one of the first and second sections; andinjecting a second injectable material flexibly distinctive from thefirst injectable material and the other of the first and second sectionsinto the chamber to alter the stabilization of the spinal motionsegment.
 35. The method of claim 34, wherein the removing and injectingare performed percutaneously.
 36. The method of claim 28, wherein one ofthe first and second sections is removable from the spacer member. 37.The method of claim 36, further comprising: monitoring the stabilizationof the spinal motion segment subsequent to the positioning of the spacermember between the upper and lower spinous processes; and replacing theremovable one of the first and second sections with a third sectionflexibly distinctive from the first and second sections to alter thestabilization of the spinal motion segment.
 38. The method of claim 37,wherein the replacing is performed percutaneously.